Organic Letters

, том 25 , издание 13 , страницы 2213-2217

Asymmetric Total Synthesis of Four Stemona Alkaloids

Тип публикации: Journal Article

Дата публикации: 2023-03-26

American Chemical Society (ACS)

Organic Letters

scimago Q1

wos Q1

white level БС1

SJR: 1.235

CiteScore: 8.7

Impact factor: 5

ISSN: 15237060, 15237052

DOI: 10.1021/acs.orglett.3c00349

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PubMed ID: 36966439

Organic Chemistry

Biochemistry

Physical and Theoretical Chemistry

Краткое описание

Asymmetric total syntheses of four Stemona alkaloids were accomplished, and among them, bisdehydrostemoninine A and stemoninine A were synthesized for the first time. Notably, these four alkaloids were divergently synthesized from a common tetracyclic intermediate, which was easily obtained from a known compound. Friedel–Crafts acylation was employed to introduce the key side chain at position C3 of Stemona alkaloids.

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Журналы

	1
Nature Communications	Nature Communications, 1, 20% Nature Communications 1 публикация, 20%
Journal of the American Chemical Society	Journal of the American Chemical Society, 1, 20% Journal of the American Chemical Society 1 публикация, 20%
Alkaloids: Chemistry and Biology	Alkaloids: Chemistry and Biology, 1, 20% Alkaloids: Chemistry and Biology 1 публикация, 20%
Organic Letters	Organic Letters, 1, 20% Organic Letters 1 публикация, 20%
Russian Chemical Reviews	Russian Chemical Reviews, 1, 20% Russian Chemical Reviews 1 публикация, 20%
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American Chemical Society (ACS)	American Chemical Society (ACS), 2, 40% American Chemical Society (ACS) 2 публикации, 40%
Springer Nature	Springer Nature, 1, 20% Springer Nature 1 публикация, 20%
Elsevier	Elsevier, 1, 20% Elsevier 1 публикация, 20%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii	Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii, 1, 20% Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii 1 публикация, 20%
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Wang X. et al. Asymmetric Total Synthesis of Four Stemona Alkaloids // Organic Letters. 2023. Vol. 25. No. 13. pp. 2213-2217.

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Wang X., Wang X., Yin G., Wang Y., Zeng Y. F., Peng Y., Zhang X., Peng X., Wang Z. Asymmetric Total Synthesis of Four Stemona Alkaloids // Organic Letters. 2023. Vol. 25. No. 13. pp. 2213-2217.

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TY - JOUR

DO - 10.1021/acs.orglett.3c00349

UR - https://pubs.acs.org/doi/10.1021/acs.orglett.3c00349

TI - Asymmetric Total Synthesis of Four Stemona Alkaloids

T2 - Organic Letters

AU - Wang, Xiaodong

AU - Wang, Xiao-Dong

AU - Yin, Gaofeng

AU - Wang, Yuqing

AU - Zeng, Yao Fu

AU - Peng, Ying

AU - Zhang, Xi

AU - Peng, Xue

AU - Wang, Zhen

PY - 2023

DA - 2023/03/26

PB - American Chemical Society (ACS)

SP - 2213-2217

IS - 13

VL - 25

PMID - 36966439

SN - 1523-7060

SN - 1523-7052

ER -

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@article{2023_Wang,

author = {Xiaodong Wang and Xiao-Dong Wang and Gaofeng Yin and Yuqing Wang and Yao Fu Zeng and Ying Peng and Xi Zhang and Xue Peng and Zhen Wang},

title = {Asymmetric Total Synthesis of Four Stemona Alkaloids},

journal = {Organic Letters},

year = {2023},

volume = {25},

publisher = {American Chemical Society (ACS)},

month = {mar},

url = {https://pubs.acs.org/doi/10.1021/acs.orglett.3c00349},

number = {13},

pages = {2213--2217},

doi = {10.1021/acs.orglett.3c00349}

}

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Wang, Xiaodong, et al. “Asymmetric Total Synthesis of Four Stemona Alkaloids.” Organic Letters, vol. 25, no. 13, Mar. 2023, pp. 2213-2217. https://pubs.acs.org/doi/10.1021/acs.orglett.3c00349.